Novel mutations causing hyperimmunoglobulin d and periodic fever syndrome
暂无分享,去创建一个
[1] T. Heike,et al. [Hyperimmunoglobulinemia D and periodic fever syndrome]. , 2011, Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology.
[2] H. Waterham,et al. Hyperimmunoglobulinemia D and periodic fever syndrome; treatment with etanercept and follow-up , 2008, Clinical Rheumatology.
[3] J. Drenth,et al. Hyperimmunoglobulinaemia D syndrome in India: report of two siblings with a novel mutation , 2006, Annals of the rheumatic diseases.
[4] H. Waterham,et al. Mutational spectrum and genotype–phenotype correlations in mevalonate kinase deficiency , 2006, Human mutation.
[5] H. Waterham,et al. Manipulation of isoprenoid biosynthesis as a possible therapeutic option in mevalonate kinase deficiency. , 2006, Arthritis and rheumatism.
[6] P. Hawkins,et al. Hereditary auto-inflammatory disorders and biologics , 2006, Springer Seminars in Immunopathology.
[7] G. Hoffmann,et al. Orphanet Journal of Rare Diseases BioMed Central Review , 2006 .
[8] H. Waterham,et al. Isoprenoid biosynthesis in hereditary periodic fever syndromes and inflammation , 2003, Cellular and Molecular Life Sciences CMLS.
[9] J. Drenth,et al. Hereditary periodic fever. , 2001, The New England journal of medicine.
[10] M. Daha,et al. Immunoglobulin D enhances the release of tumour necrosis factor‐α, and interleukin‐1β as well as interleukin‐1 receptor antagonist from human mononuclear cells , 1996, Immunology.
[11] K. Sartor,et al. Clinical and biochemical phenotype in 11 patients with mevalonic aciduria. , 1993, Pediatrics.